Citation

BibTex format

@article{Bertheleme:2014:10.1371/journal.pone.0089613,
author = {Bertheleme, N and Strege, A and Bunting, SE and Dowell, SJ and Byrne, B},
doi = {10.1371/journal.pone.0089613},
journal = {PLoS One},
pages = {1--10},
title = {Arginine 199 and leucine 208 have key roles in the control of adenosine A(2A) receptor signalling function},
url = {http://dx.doi.org/10.1371/journal.pone.0089613},
volume = {9},
year = {2014}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - One successful approach to obtaining high-resolution crystal structures of G-protein coupled receptors is the introduction of thermostabilising mutations within the receptor. This technique allows the generation of receptor constructs stabilised into different conformations suitable for structural studies. Previously, we functionally characterised a number of mutants of the adenosine A2A receptor, thermostabilised either in an agonist or antagonist conformation, using a yeast cell growth assay and demonstrated that there is a correlation between thermostability and loss of constitutive activity. Here we report the functional characterisation of 30 mutants intermediate between the Rag23 (agonist conformation mutant) and the wild-type receptor using the same yeast signalling assay with the aim of gaining greater insight into the role individual amino acids have in receptor function. The data showed that R199 and L208 have important roles in receptor function; substituting either of these residues for alanine abolishes constitutive activity. In addition, the R199A mutation markedly reduces receptor potency while L208A reduces receptor efficacy. A184L and L272A mutations also reduce constitutive activity and potency although to a lesser extent than the R199A and L208A. In contrast, the F79A mutation increases constitutive activity, potency and efficacy of the receptor. These findings shed new light on the role individual residues have on stability of the receptor and also provide some clues as to the regions of the protein responsible for constitutive activity. Furthermore, the available adenosine A2A receptor structures have allowed us to put our findings into a structural context.
AU - Bertheleme,N
AU - Strege,A
AU - Bunting,SE
AU - Dowell,SJ
AU - Byrne,B
DO - 10.1371/journal.pone.0089613
EP - 10
PY - 2014///
SN - 1932-6203
SP - 1
TI - Arginine 199 and leucine 208 have key roles in the control of adenosine A(2A) receptor signalling function
T2 - PLoS One
UR - http://dx.doi.org/10.1371/journal.pone.0089613
UR - http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332468900025&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
UR - https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0089613
UR - http://hdl.handle.net/10044/1/94015
VL - 9
ER -

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